Investigation of the Scope of Heterogeneous and Homogeneous Procedures for Preparing Magnesium Chelates of Porphyrins, Hydroporphyrins, and Phthalocyanines
- 1 January 1996
- journal article
- Published by American Chemical Society (ACS) in Inorganic Chemistry
- Vol. 35 (25) , 7325-7338
- https://doi.org/10.1021/ic960812p
Abstract
A simple method has been developed for metalation of porphyrinic compounds under homogeneous conditions at room temperature using a stable ethereal solution of MgI2 and N,N-diisopropylethylamine. A previously developed heterogeneous procedure employs a mixture of a magnesium halide and a nonnucleophilic amine in a noncoordinating solvent at room temperature. The scope of the heterogeneous and homogeneous magnesium insertion procedures has been investigated across a family of 19 porphyrinic compounds, including synthetic porphyrins, synthetic or naturally occurring chlorins, and organic-soluble phthalocyanines. The rate of magnesium insertion increased in the series phthalocyanines < chlorins < porphyrins, which parallels the basicity of the ligands. Though phthalocyanines have the smallest core size, the magnesium phthalocyanines were far more stable than magnesium porphyrins to acid-induced demetalation. The heterogeneous method is broadly applicable to porphyrins, chlorins, and phthalocyanines. The homogeneous method is generally slower than the heterogeneous method, though both afford rapid metalation of most porphyrins, including electron-deficient, peripherally coordinating, or facially encumbered meso-substituted tetraarylporphyrins, and the β-substituted octaethylporphyrin. Chlorin e6 trimethyl ester and methyl pyropheophorbide a were metalated cleanly under homogeneous but not heterogeneous conditions, while pheophytin a failed with both methods. The homogeneous method failed altogether with phthalocyanines. Several methods in magnesium chemistry have been developed that augment these procedures, including a mild synthesis of tetraphenylchlorin and a streamlined separation of porphyrin, chlorin, and bacteriochlorins based on selective formation of the magnesium chelates. Collectively, these methods should broaden the scope of model systems based on magnesium chelates of porphyrinic compounds.Keywords
This publication has 40 references indexed in Scilit:
- Two-photon excitation of alkyl-substituted magnesium phthalocyanine: radical formation via higher excited statesJournal of Photochemistry and Photobiology A: Chemistry, 1994
- 2,3‐Dihydroporphycene–an Analogue of ChlorinAngewandte Chemie International Edition in English, 1987
- Crystal and molecular structure of the isobacteriochlorin 3,7-dimethyl-3',7'-dihydro-2,2',8,8',12,13,17,18-octaethylporphyrin. A model for sirohydrochlorin and sirohemeJournal of the American Chemical Society, 1982
- Equilibrium constants for the metalation of zinc porphyrinsInorganic Chemistry, 1977
- On the preparation of metalloporphyrinsJournal of Inorganic and Nuclear Chemistry, 1970
- Structure of aquomagnesium tetraphenylporphyrinJournal of the American Chemical Society, 1969
- Dipole Moments of PhenylmercurialsJournal of the American Chemical Society, 1955
- The Diffusion Coefficient of Cupric GlycinateJournal of the American Chemical Society, 1952
- Studies in the Chlorophyll Series. XIV. Potentiometric Titration in Acetic Acid Solution of the Basic Groups in Chlorophyll Derivatives1Journal of the American Chemical Society, 1934
- Synthese des Hämatoporphyrins, Protoporphyrins und HäminsEuropean Journal of Organic Chemistry, 1929